Canonical Allele Identifier: CA2349705276
Gene: SNAP25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10239928_10239933del , CM000682.2:g.10239928_10239933del GRCh38
NC_000020.10:g.10220576_10220581del , CM000682.1:g.10220576_10220581del GRCh37
NC_000020.9:g.10168576_10168581del NCBI36
NG_029626.1:g.26100_26105del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706269.1:c.-64+20715_-64+20720del ENSP00000516314.1:n.-64+20715_-64+20720del
ENST00000685131.1:c.-64+1902_-64+1907del ENSP00000508837.1:n.-64+1902_-64+1907del
ENST00000687785.1:c.-241-4047_-241-4042del ENSP00000510219.1:n.-241-4047_-241-4042del
ENST00000689077.1:n.393-35501_393-35496del
ENST00000689248.1:n.97-4824_97-4819del
ENST00000689757.1:c.-109+12490_-109+12495del ENSP00000509312.1:n.-109+12490_-109+12495del
ENST00000689858.1:c.-123-4047_-123-4042del ENSP00000510663.1:n.-123-4047_-123-4042del
ENST00000690099.1:n.393-35501_393-35496del
ENST00000690766.1:n.393-35501_393-35496del
ENST00000690812.1:c.-168-4047_-168-4042del ENSP00000509287.1:n.-168-4047_-168-4042del
ENST00000691161.1:c.-64+12490_-64+12495del ENSP00000510109.1:n.-64+12490_-64+12495del
ENST00000691353.1:c.-263+20715_-263+20720del ENSP00000509759.1:n.-263+20715_-263+20720del
ENST00000691665.1:c.-64+5591_-64+5596del ENSP00000508541.1:n.-64+5591_-64+5596del
ENST00000692411.1:c.-149+20951_-149+20956del ENSP00000508939.1:n.-149+20951_-149+20956del
ENST00000693325.1:c.-64+12490_-64+12495del ENSP00000510558.1:n.-64+12490_-64+12495del
ENST00000693732.1:n.393-35501_393-35496del
ENST00000254976.7:c.-64+20951_-64+20956del MANE Select ENSP00000254976.3:n.-64+20951_-64+20956del
ENST00000254976.6:c.-64+20951_-64+20956del ENSP00000254976.2:n.-64+20951_-64+20956del
ENST00000304886.6:c.-64+20951_-64+20956del ENSP00000307341.2:n.-64+20951_-64+20956del
ENST00000430336.1:c.-64+20715_-64+20720del ENSP00000400720.1:n.-64+20715_-64+20720del
NM_003081.3:c.-64+20951_-64+20956del NP_003072.2:n.-64+20951_-64+20956del
NM_130811.2:c.-64+20951_-64+20956del NP_570824.1:n.-64+20951_-64+20956del
XM_005260808.3:c.-64+20715_-64+20720del XP_005260865.1:n.-64+20715_-64+20720del
XM_005260810.3:c.-64+20715_-64+20720del XP_005260867.1:n.-64+20715_-64+20720del
NM_001322902.1:c.-64+20715_-64+20720del NP_001309831.1:n.-64+20715_-64+20720del
NM_001322903.1:c.-64+5591_-64+5596del NP_001309832.1:n.-64+5591_-64+5596del
NM_001322904.1:c.-64+12490_-64+12495del NP_001309833.1:n.-64+12490_-64+12495del
NM_001322905.1:c.-123-4047_-123-4042del NP_001309834.1:n.-123-4047_-123-4042del
NM_001322906.1:c.-64+1902_-64+1907del NP_001309835.1:n.-64+1902_-64+1907del
NM_001322907.1:c.-64+12490_-64+12495del NP_001309836.1:n.-64+12490_-64+12495del
NM_001322908.1:c.-241-4047_-241-4042del NP_001309837.1:n.-241-4047_-241-4042del
NM_001322909.1:c.-108-19429_-108-19424del NP_001309838.1:n.-108-19429_-108-19424del
NM_001322910.1:c.-64+12490_-64+12495del NP_001309839.1:n.-64+12490_-64+12495del
NM_003081.4:c.-64+20951_-64+20956del NP_003072.2:n.-64+20951_-64+20956del
NM_130811.3:c.-64+20951_-64+20956del NP_570824.1:n.-64+20951_-64+20956del
XM_005260808.5:c.-64+20715_-64+20720del XP_005260865.1:n.-64+20715_-64+20720del
XM_017028021.2:c.-123-4047_-123-4042del XP_016883510.1:n.-123-4047_-123-4042del
XM_017028022.1:c.-64+1902_-64+1907del XP_016883511.1:n.-64+1902_-64+1907del
NM_001322902.2:c.-64+20715_-64+20720del NP_001309831.1:n.-64+20715_-64+20720del
NM_001322903.2:c.-64+5591_-64+5596del NP_001309832.1:n.-64+5591_-64+5596del
NM_001322904.2:c.-64+12490_-64+12495del NP_001309833.1:n.-64+12490_-64+12495del
NM_001322905.2:c.-123-4047_-123-4042del NP_001309834.1:n.-123-4047_-123-4042del
NM_001322906.2:c.-64+1902_-64+1907del NP_001309835.1:n.-64+1902_-64+1907del
NM_001322907.2:c.-64+12490_-64+12495del NP_001309836.1:n.-64+12490_-64+12495del
NM_001322908.2:c.-241-4047_-241-4042del NP_001309837.1:n.-241-4047_-241-4042del
NM_001322909.2:c.-108-19429_-108-19424del NP_001309838.1:n.-108-19429_-108-19424del
NM_001322910.2:c.-64+12490_-64+12495del NP_001309839.1:n.-64+12490_-64+12495del
NM_003081.5:c.-64+20951_-64+20956del NP_003072.2:n.-64+20951_-64+20956del
NM_130811.4:c.-64+20951_-64+20956del MANE Select NP_570824.1:n.-64+20951_-64+20956del